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  5. NDC Package Code: 51801-779-08 Amcon Labs Hand Sanitizer Light Cleansing

NDC Package 51801-779-08 Amcon Labs Hand Sanitizer Light Cleansing

Alcohol Spray Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
51801-779-08
Package Description:
.237 L in 1 BOTTLE, PUMP
Product Code:
51801-779
Proprietary Name:
Amcon Labs Hand Sanitizer Light Cleansing
Non-Proprietary Name:
Alcohol
Substance Name:
Alcohol
Usage Information:
Dispense a small amount of spray onto the hands.Spread on hands and rub into skin until dry.Dispense a smaller amount in one hand and spread over both hands and wrists.Rub into skin until dry.Children should be supervised while using this product.
11-Digit NDC Billing Format:
51801077908
NDC to RxNorm Crosswalk:
  • RxCUI: 1367692 - ethanol 60 % Topical Spray
  • RxCUI: 1367692 - ethanol 0.6 ML/ML Topical Spray
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Nomax, Inc.
    Dosage Form:
    Spray - A liquid minutely divided as by a jet of air or steam.
    Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Active Ingredient(s):
  • ALCOHOL 600 mL/L
    • Sample Package:
    No
    FDA Application Number:
    505G(a)(3)
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    08-04-2023
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 51801-779-08?

    The NDC Packaged Code 51801-779-08 is assigned to a package of .237 l in 1 bottle, pump of Amcon Labs Hand Sanitizer Light Cleansing, a human over the counter drug labeled by Nomax, Inc.. The product's dosage form is spray and is administered via topical form.

    Is NDC 51801-779 included in the NDC Directory?

    Yes, Amcon Labs Hand Sanitizer Light Cleansing with product code 51801-779 is active and included in the NDC Directory. The product was first marketed by Nomax, Inc. on August 04, 2023 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 51801-779-08?

    The 11-digit format is 51801077908. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-251801-779-085-4-251801-0779-08